Reaktion #1835692

ord-abeb5c6f102849b8a73a079526879e11

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigedescribed in Reference Example 82 at room temperature
  2. 2
    SonstigeAfter completion of the reaction
  3. 3
    Sonstigethe solvent and trifluoroacetic acid were evaporated
  4. 4
    Sonstigethe resulting residue was purified with silica gel column chromatography (n-hexane/ethyl acetate)

Vorschrift

Trifluoroacetic acid (4.1 ml) was added to 8-(5-bromopyridin-2-yl)-1,4-dioxaspiro[4,5]decane-8-carbonitrile (3.4 g) described in Reference Example 82 at room temperature, and stirred at the same temperature for 22 hours. After completion of the reaction, the solvent and trifluoroacetic acid were evaporated and the resulting residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give 1-(5-bromopyridin-2-yl)-4-oxocyclohexanecarbonitrile (2.78 g) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09150555B2uspto-grants-2015_10